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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837758Generated: November 1, 2026

Dimethylformamide → N1-(3-Fluorobenzyl)-2-[1-[2-[1-(cyclopropylmethyl)-2-oxo-1,2-dihydro-3-pyridinyl]ethyl]-2-piperidyl]acetamide

https://huagongshe.com/reaction/1837758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
ReactantN1-(3-Fluorobenzyl)-2-[1-[2-(2-oxo-1,2-dihydro-3-pyridinyl)ethyl]-2-piperidyl]acetamideHCID 22678298—
SolventWaterHCID 962—
ProductN1-(3-Fluorobenzyl)-2-[1-[2-[1-(cyclopropylmethyl)-2-oxo-1,2-dihydro-3-pyridinyl]ethyl]-2-piperidyl]acetamideHCID 22678543—

Reaction Steps

230 mg of N1-(3-fluorobenzyl)-2-[1-[2-(2-oxo-1,2-dihydro-3-pyridinyl)ethyl]-2-piperidyl]acetamide obtained in Example 198, 0.08 ml of cyclopropylmethyl chloride, 450 mg of potassium carbonate and 5 ml of DMF were stirred at 60° C. for 1 hour. Water was added thereto, and the mixture was extracted with ethyl acetate. The extract was dried over sodium sulfate. The drying agent was filtered off, and the solvent was evaporated. The residue was purified by NH-silica gel column chromatography (hexane:ethyl acetate=1:1, subsequently ethyl acetate), to give 180 mg of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-67a8a4aa8c98467b876e4634ec38b19c
Source noteuspto-grants-2004_08